RU2397182C2 - Микрогели в сшиваемой органической среде, способ их получения и их применение - Google Patents
Микрогели в сшиваемой органической среде, способ их получения и их применение Download PDFInfo
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- RU2397182C2 RU2397182C2 RU2006114345/04A RU2006114345A RU2397182C2 RU 2397182 C2 RU2397182 C2 RU 2397182C2 RU 2006114345/04 A RU2006114345/04 A RU 2006114345/04A RU 2006114345 A RU2006114345 A RU 2006114345A RU 2397182 C2 RU2397182 C2 RU 2397182C2
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- microgel
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Classifications
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/075—Macromolecular gels
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2220/00—Compositions for preparing gels other than hydrogels, aerogels and xerogels
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- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyurethanes Or Polyureas (AREA)
- Polymerisation Methods In General (AREA)
- Paints Or Removers (AREA)
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2616001C2 (ru) * | 2012-11-06 | 2017-04-12 | Ппг Индастриз Огайо, Инк. | Неводные дисперсии, содержащие акриловый полимерный стабилизатор и затравочный полимер, стабилизированный с использованием алифатического сложного полиэфира |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6956084B2 (en) * | 2001-10-04 | 2005-10-18 | Bridgestone Corporation | Nano-particle preparation and applications |
DE10344975A1 (de) * | 2003-09-27 | 2005-04-21 | Rhein Chemie Rheinau Gmbh | Mikrogele in nicht-vernetzbaren organischen Medien |
DE10345043A1 (de) * | 2003-09-27 | 2005-04-21 | Rhein Chemie Rheinau Gmbh | Mikrogel-enthaltende Zusammensetzung |
US7205370B2 (en) | 2004-01-12 | 2007-04-17 | Bridgestone Corporation | Polymeric nano-particles of flower-like structure and applications |
US8063142B2 (en) | 2004-03-02 | 2011-11-22 | Bridgestone Corporation | Method of making nano-particles of selected size distribution |
US7718737B2 (en) | 2004-03-02 | 2010-05-18 | Bridgestone Corporation | Rubber composition containing functionalized polymer nanoparticles |
US20050282956A1 (en) | 2004-06-21 | 2005-12-22 | Xiaorong Wang | Reversible polymer/metal nano-composites and method for manufacturing same |
US7998554B2 (en) | 2004-07-06 | 2011-08-16 | Bridgestone Corporation | Hydrophobic surfaces with nanoparticles |
DE102004062551A1 (de) * | 2004-12-24 | 2006-07-06 | Rhein Chemie Rheinau Gmbh | Mikrogel-enthaltende duroplastische Zusammensetzung |
US7659342B2 (en) | 2005-02-03 | 2010-02-09 | Bridgestone Corporation | Polymer nano-particle with polar core and method for manufacturing same |
DE102005014270A1 (de) | 2005-03-24 | 2006-10-05 | Rhein Chemie Rheinau Gmbh | Verwendung von vernetzten Mikrogelen zur Modifikation des temperaturabhängigen Verhaltens von nicht-vernetzbaren organischen Medien |
DE102005014272A1 (de) | 2005-03-24 | 2006-09-28 | Rhein Chemie Rheinau Gmbh | Mikrogele und Verdickungsmittel enthaltende Zusammensetzungen |
US7947782B2 (en) | 2005-05-16 | 2011-05-24 | Rhein Chemie Rheinau Gmbh | Microgel-containing vulcanisable composition |
US7538159B2 (en) * | 2005-12-16 | 2009-05-26 | Bridgestone Corporation | Nanoparticles with controlled architecture and method thereof |
US9061900B2 (en) | 2005-12-16 | 2015-06-23 | Bridgestone Corporation | Combined use of liquid polymer and polymeric nanoparticles for rubber applications |
US7884160B2 (en) | 2005-12-19 | 2011-02-08 | Bridgestone Corporation | Non-spherical nanoparticles made from living triblock polymer chains |
US8288473B2 (en) | 2005-12-19 | 2012-10-16 | Bridgestone Corporation | Disk-like nanoparticles |
US8697775B2 (en) | 2005-12-20 | 2014-04-15 | Bridgestone Corporation | Vulcanizable nanoparticles having a core with a high glass transition temperature |
US8877250B2 (en) | 2005-12-20 | 2014-11-04 | Bridgestone Corporation | Hollow nano-particles and method thereof |
EP1889735B1 (en) * | 2006-07-26 | 2009-09-16 | Sumitomo Rubber Industries, Ltd. | Rubber composition and tire using same |
US8541503B2 (en) | 2006-07-28 | 2013-09-24 | Bridgestone Corporation | Polymeric core-shell nanoparticles with interphase region |
US7597959B2 (en) | 2006-12-19 | 2009-10-06 | Bridgestone Corporation | Core-shell fluorescent nanoparticles |
US7649049B2 (en) | 2006-12-20 | 2010-01-19 | Bridgestone Corporation | Rubber composition containing a polymer nanoparticle |
JP5214886B2 (ja) * | 2007-01-12 | 2013-06-19 | 東洋ゴム工業株式会社 | 空気入りタイヤ |
JP5214887B2 (ja) * | 2007-01-17 | 2013-06-19 | 東洋ゴム工業株式会社 | 空気入りタイヤ |
JP5214888B2 (ja) * | 2007-01-17 | 2013-06-19 | 東洋ゴム工業株式会社 | 空気入りタイヤ |
DE102007011424A1 (de) | 2007-03-08 | 2008-09-11 | Lanxess Deutschland Gmbh | Polymerelektrolytmembran mit funktionalisierten Nanopartikeln |
DE102007020451A1 (de) * | 2007-04-27 | 2008-10-30 | Lanxess Deutschland Gmbh | Verfahren zur Herstellung von Kautschukmischungen |
US7829624B2 (en) | 2007-06-29 | 2010-11-09 | Bridgestone Corporation | One-pot synthesis of nanoparticles and liquid polymer for rubber applications |
JP5248082B2 (ja) * | 2007-10-22 | 2013-07-31 | 東洋ゴム工業株式会社 | 空気入りタイヤ用ゴム組成物 |
WO2009141391A1 (de) * | 2008-05-23 | 2009-11-26 | Rhein Chemie Rheinau Gmbh | Kohlenstoffnanoröhren und mikrogele enthaltende organische medien |
DE102008056975A1 (de) | 2008-11-13 | 2010-05-20 | Lanxess Deutschland Gmbh | Lagerstabile, hydroxylmodifizierte Mikrogellatices |
EP2370349B1 (en) | 2008-12-31 | 2014-10-29 | Bridgestone Corporation | Core-first nanoparticle formation process, nanoparticle, and composition |
US9062144B2 (en) | 2009-04-03 | 2015-06-23 | Bridgestone Corporation | Hairy polymeric nanoparticles with first and second shell block polymer arms |
DE102009060440A1 (de) * | 2009-12-22 | 2011-06-30 | nora systems GmbH, 69469 | Verfahren zur Herstellung eines flächenförmigen Gummibelags und flächenförmiger Gummibelag |
US9115222B2 (en) | 2009-12-29 | 2015-08-25 | Bridgestone Corporation | Well defined, highly crosslinked nanoparticles and method for making same |
JP5809633B2 (ja) * | 2010-09-30 | 2015-11-11 | 株式会社カネカ | 分岐高分子を含有する制振材料用組成物 |
JP5800659B2 (ja) * | 2011-10-05 | 2015-10-28 | オリンパス株式会社 | 医療器具用接着剤組成物、および内視鏡装置 |
US9428604B1 (en) | 2011-12-30 | 2016-08-30 | Bridgestone Corporation | Nanoparticle fillers and methods of mixing into elastomers |
CN103450400B (zh) * | 2012-06-01 | 2015-07-29 | 中国石油天然气股份有限公司 | 一种乳液聚合法制备羧基丁腈橡胶的方法 |
EP2796503B1 (de) | 2013-04-26 | 2016-03-02 | LANXESS Deutschland GmbH | Zusammensetzungen, enthaltend Thermoplasten auf Basis von Polyvinylchlorid sowie mit Hydroxylgruppen modifizierte, vernetzte NBR-Mikrogele |
JP2018506152A (ja) | 2015-02-04 | 2018-03-01 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | 導電性ペースト組成物およびそれによって製造された半導体デバイス |
CA3035729A1 (en) | 2016-09-02 | 2018-03-08 | The Willamette Valley Company | Polymeric composition comprising spherical aggregate and method of use thereof |
CN110964593B (zh) * | 2019-12-18 | 2021-06-01 | 中国科学院兰州化学物理研究所 | 一种聚合诱导自组装油凝胶及其制备方法和应用 |
Family Cites Families (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2187146A (en) * | 1936-10-24 | 1940-01-16 | Du Pont | Process of coagulation |
US4055607A (en) | 1972-10-11 | 1977-10-25 | Ppg Industries, Inc. | Acrylic coating compositions |
US3880796A (en) * | 1972-10-11 | 1975-04-29 | Ppg Industries Inc | Method of making a nonaqueous acrylic coating composition |
US4025474A (en) | 1975-06-02 | 1977-05-24 | Ppg Industries, Inc. | Polyester coating compositions comprising cross-linked polymeric microparticles |
US4115472A (en) | 1975-03-19 | 1978-09-19 | Ppg Industries, Inc. | Urethane coating compositions |
GB1588978A (en) | 1977-07-19 | 1981-05-07 | Ici Ltd | Coating processes |
DE2910168A1 (de) * | 1979-03-15 | 1980-09-25 | Bayer Ag | Kautschukdispersionen |
US4533598A (en) * | 1983-11-18 | 1985-08-06 | Caschem, Inc. | Extended polyurethanes |
US5238977A (en) * | 1987-12-12 | 1993-08-24 | Bayer Aktiengesellschaft | Graft polymer dispersions |
DE3743486A1 (de) * | 1987-12-22 | 1989-07-13 | Bayer Ag | Weiche, thermoplastisch verarbeitbare, polyamid enthaltende polymerlegierungen |
US5013793A (en) * | 1990-07-26 | 1991-05-07 | Exxon Chemical Patents Inc. | Dynamically cured thermoplastic olefin polymers and process for producing the same |
US5229434A (en) * | 1988-12-20 | 1993-07-20 | Toyo Ink Manufacturing Co., Ltd. | Process for the production of reactive microgel and resin composition containing the microgel |
US5302696A (en) * | 1989-05-16 | 1994-04-12 | Olin Corporation | Process for minimizing residual free hydrazine in polymer latices |
DE3920745A1 (de) * | 1989-06-24 | 1991-01-03 | Bayer Ag | Kautschukmischungen enthaltend schwefel-modifizierte polychloroprengel |
JP3031022B2 (ja) * | 1991-12-19 | 2000-04-10 | 住友化学工業株式会社 | 熱可塑性エラストマー組成物の製造方法 |
DE4220563A1 (de) * | 1992-06-24 | 1994-01-13 | Bayer Ag | Kautschukmischungen enthaltend Polybutadien-Gel |
EP0656388B1 (fr) * | 1993-11-26 | 2001-04-11 | Atofina | Alliages de thermoplastique et caoutchouc adhérents sur des thermoplastiques |
US5424356A (en) * | 1994-03-21 | 1995-06-13 | The Goodyear Tire & Rubber Company | Process for the preparation of hydrogenated rubber |
DE19701488A1 (de) * | 1997-01-17 | 1998-07-23 | Bayer Ag | SBR-Kautschukgele enthaltende Kautschukmischungen |
DE19701489A1 (de) * | 1997-01-17 | 1998-07-23 | Bayer Ag | Modifizierte Kautschukgele enthaltende Kautschukmischungen |
US6136923A (en) * | 1997-10-15 | 2000-10-24 | The Dow Chemical Company | Thermoplastic compositions of interpolymers of ethylene with styrene blended with poly vinyl chloride |
US5976232A (en) * | 1998-04-30 | 1999-11-02 | Hewlett-Packard Company | Homogenization process for ink-jet inks containing fine dispersions of pigments |
DE19834803A1 (de) * | 1998-08-01 | 2000-02-03 | Continental Ag | Kautschukmischung |
DE19834804A1 (de) * | 1998-08-01 | 2000-02-03 | Continental Ag | Kautschukmischung |
DE19834802A1 (de) * | 1998-08-01 | 2000-02-03 | Continental Ag | Kautschukmischung |
WO2000061662A1 (fr) * | 1999-04-13 | 2000-10-19 | Asahi Kasei Kogyo Kabushiki Kaisha | Procédé de production d'une composition à base de caoutchouc |
DE19919459A1 (de) * | 1999-04-29 | 2000-11-02 | Rheinchemie Rheinau Gmbh | Polyurethan-Kautschukmischungen enthaltend modifizierte Kautschukgele |
EP1063259A1 (de) * | 1999-06-26 | 2000-12-27 | Bayer Ag | Mikrogelhaltige Kautschukcompounds mit schwefelhaltigen Organosiliciumverbindungen |
DE19939865A1 (de) * | 1999-08-23 | 2001-03-01 | Bayer Ag | Agglomerierte Kautschukgele enthaltende Kautschukmischungen und Vulkanisate |
DE19942620A1 (de) * | 1999-09-07 | 2001-03-08 | Bayer Ag | Mikrogelhaltige Kautschukmischungen mit verkappten bifunktionellen Mercaptanen und hieraus hergestellte Vulkanisate |
EP1083169B1 (de) * | 1999-09-07 | 2003-10-29 | Bayer Ag | Funktionalisierte Alkoxyamin-Initiatoren |
EP1262510B1 (en) * | 1999-12-03 | 2007-02-07 | China Petro-Chemical Corporation | Full vulcanized powdered rubber with controllable particle diameter, preparing method and uses thereof |
DE19962862A1 (de) * | 1999-12-24 | 2001-06-28 | Bayer Ag | Kautschukmischungen auf Basis von unvernetzten Kautschuken und vernetzten Kautschukpartikeln sowie multifunktionellen Isocyanaten |
DE10021070A1 (de) * | 2000-04-28 | 2001-10-31 | Bayer Ag | Gelhaltige Kautschukmischungen für dynamisch belastete Reifenbauteile |
CN1330095A (zh) * | 2000-06-15 | 2002-01-09 | 中国石油化工股份有限公司 | 一种全硫化热塑性弹性体及其制备方法 |
DE10038488A1 (de) * | 2000-08-08 | 2002-02-21 | Bayer Ag | Isocyanatosilan- und mikrogelhaltige Kautschukmischungen |
DE10039749A1 (de) * | 2000-08-16 | 2002-02-28 | Bayer Ag | Kautschukmischungen auf Basis von unvernetzten Kautschuken und vernetzten Kautschukpartikeln sowie multifunktionellen Isocyanaten auf Polyuretbasis |
DE10052287A1 (de) * | 2000-10-20 | 2002-04-25 | Bayer Ag | Kautschukgele und Phenolharzedukte enthaltende Kautschukmischungen |
DE10054533A1 (de) * | 2000-11-03 | 2002-05-08 | Bayer Ag | Mikrogelhaltige Kautschukmischungen mit Phoshorylpolysulfiden und hieraus hergestellte Vulkanisate bzw. Formkörper |
DE10056311A1 (de) * | 2000-11-14 | 2002-05-16 | Bayer Ag | Gelhaltige Kautschukmischungen mit anorganischen Peroxiden |
DE10061174A1 (de) * | 2000-12-07 | 2002-06-20 | Bayer Ag | NBR-Gele in Butylkautschukcompounds |
DE10061543A1 (de) * | 2000-12-11 | 2002-06-13 | Bayer Ag | Gelhaltige Kautschukmischungen mit multifunktionellen Isocyanaten und Polyolen |
CN1177895C (zh) * | 2001-10-12 | 2004-12-01 | 中国石油化工股份有限公司 | 一种增韧热固性树脂及其制备方法 |
DE10212391B4 (de) * | 2002-03-20 | 2006-11-16 | Mankiewicz Gebr. & Co (Gmbh & Co Kg) | Zweikomponenten-Zusammensetzung zur Herstellung von Polyurethan-Gelcoats |
DE10344975A1 (de) * | 2003-09-27 | 2005-04-21 | Rhein Chemie Rheinau Gmbh | Mikrogele in nicht-vernetzbaren organischen Medien |
DE10345043A1 (de) * | 2003-09-27 | 2005-04-21 | Rhein Chemie Rheinau Gmbh | Mikrogel-enthaltende Zusammensetzung |
-
2003
- 2003-09-27 DE DE10344976A patent/DE10344976A1/de not_active Withdrawn
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2004
- 2004-09-23 JP JP2006527424A patent/JP2007506832A/ja not_active Withdrawn
- 2004-09-23 US US10/947,875 patent/US20050182158A1/en not_active Abandoned
- 2004-09-23 CA CA2539499A patent/CA2539499C/en active Active
- 2004-09-23 RU RU2006114345/04A patent/RU2397182C2/ru active
- 2004-09-23 US US10/573,217 patent/US20070232733A1/en not_active Abandoned
- 2004-09-23 BR BRPI0414789-8A patent/BRPI0414789A/pt not_active Application Discontinuation
- 2004-09-23 EP EP04766849.6A patent/EP1664158B1/de active Active
- 2004-09-23 WO PCT/EP2004/052294 patent/WO2005033186A1/de active Application Filing
- 2004-09-23 CN CN2004800279137A patent/CN1856528B/zh active Active
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2013
- 2013-02-08 JP JP2013023835A patent/JP5766224B2/ja not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
Энциклопедия полимеров. - М.: Советская энциклопедия, 1972, т.1, кол.595. * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2616001C2 (ru) * | 2012-11-06 | 2017-04-12 | Ппг Индастриз Огайо, Инк. | Неводные дисперсии, содержащие акриловый полимерный стабилизатор и затравочный полимер, стабилизированный с использованием алифатического сложного полиэфира |
Also Published As
Publication number | Publication date |
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WO2005033186A1 (de) | 2005-04-14 |
DE10344976A1 (de) | 2005-04-21 |
CN1856528B (zh) | 2012-11-14 |
EP1664158A1 (de) | 2006-06-07 |
CN1856528A (zh) | 2006-11-01 |
CA2539499C (en) | 2012-12-18 |
RU2006114345A (ru) | 2007-11-10 |
US20050182158A1 (en) | 2005-08-18 |
JP2013136764A (ja) | 2013-07-11 |
JP2007506832A (ja) | 2007-03-22 |
BRPI0414789A (pt) | 2006-11-21 |
JP5766224B2 (ja) | 2015-08-19 |
US20070232733A1 (en) | 2007-10-04 |
EP1664158B1 (de) | 2019-05-01 |
WO2005033186A9 (de) | 2005-06-09 |
CA2539499A1 (en) | 2005-04-14 |
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